Multimedical s.r.l.
IT-MF-000020128 · Italy · Viadana
Multimedical s.r.l. is registered in the European database on medical devices as a manufacturer, with 242 devices declared. It has a similarly named entry in the FDA register that we have not verified.
What this manufacturer declares
| Class IIa | 242 |
|---|
Most frequent device types declared: ACCESSORI PER INFUSIONE, AGO DI HUBER, CANULA CHIRURGICA, DEFLUSSORE PER IRRIGAZIONE ARTROSCOPICA, DEFLUSSORE UROLOGICO.
Among these devices, 242 are declared sterile, 2 active.
Devices declared under this manufacturer
- AGO DI HUBER
- MICRON FILTER
- MINI SPIKE CHEMO
- MINISPIKE-CRN
- PROFILL -CRN
- RAMPA
- RAMPA HP
- SOFT ELASPUMP
- SPIKE CHEMO
- TAPPO LUER LOCK
- TRANSFUSET
- TRANSFUSET DEHP FREE
Showing 12 of 242 declared devices.
Catalogue references include 090405/ND, 090780/1/FF, 090780/HP/R/OFF, 090781/1/FF, 090830/1930/M, 090833/2015.
European nomenclature codes declared: A01010302, A0704, A03010102, A0702, A0703, A070103.
United States market access
| FDA establishment register | Similar name found — unverified |
|---|---|
| Matched entry | MULTIMEDICAL SRL (IT) · FDA 8021079 |
| Devices in EUDAMED | 242 |
| Country of registration | Italy |
⚠️ A similar name exists; we do not assert it is the same company — why.
Device-level evidence
| Devices with a numeric GTIN | 242 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
0425-MDR-030202-00 | issued | 2031-06-25 |
0425-MDR-030201-00 | issued | 2031-06-25 |